Evidence map›Paper›PMID 41675658›Full record

ArticleQuantitative biology (Beijing, China)2023

Cell-based allometry: an approach for evaluation of complexity in morphogenesis.

Ali Tarihi, Mojtaba Tarihi, Taki Tiraihi

Abstract read
In one paragraph

Article in Quantitative biology (Beijing, China), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Ali TarihiDepartment of Computer Engineering Faculty of Computer Science and Engineering Shahid Behshti University Tehran 19839-69411 Iran.
Mojtaba TarihiDepartment of Computer Engineering Sharif University of Technology Tehran 11365-11155 Iran.
Taki TiraihiDepartment of Anatomical Sciences School of Medical Sciences Tarbiat Modares University Tehran 14117-13116 Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Morphogenesis is a complex process in a developing animal at the organ, cellular and molecular levels. In this investigation, allometry at the cellular level was evaluated. Methods: Geometric information, including the time-lapse Cartesian coordinates of each cell's center, was used for calculating the allometric coefficients. A zero-centroaxial skew-symmetrical matrix ( Results: We explored two out of the four first generated blastomeres in Conclusion: The conclusion of this study is that the complexity of the differentiating cells in a developing embryo can be evaluated by allometric scaling based on the data derived from the Cartesian coordinates of the cells at different stages of development.

Indexed as

allometrybioinformaticsC. eleganscomplexityembryogenesismorphogenesisskew matrix

Identifiers

PMID41675658
PMCPMC12807192

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.